A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045259



Internal ID19134478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54953335..55283986hg38UCSC Ensembl
Innerchr11:54720811..55051462hg19UCSC Ensembl
Innerchr11:54477387..54808038hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38330652
hg19330652
hg18330652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1163n100
Supporting Variantsnssv3509938, nssv3503740
Samples
Known GenesTRIM48
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045259
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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